endometriosis; Gene Set

Dataset	GAD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	The growth of functional endometrial tissue in anatomic sites outside the uterine body. It most often occurs in the pelvic organs. (Experimental Factor Ontology, EFO_0001065)
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Genes

13 genes associated with the disease endometriosis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol	Name
CYP1B1	cytochrome P450, family 1, subfamily B, polypeptide 1
CYP2C19	cytochrome P450, family 2, subfamily C, polypeptide 19
ESR2	estrogen receptor 2 (ER beta)
HLA-A	major histocompatibility complex, class I, A
HLA-B	major histocompatibility complex, class I, B
IL10	interleukin 10
MEGF10	multiple EGF-like-domains 10
MMP2	matrix metallopeptidase 2
PGR	progesterone receptor
PTPN22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SERPINE1	serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
TIMP2	TIMP metallopeptidase inhibitor 2
VEGFA	vascular endothelial growth factor A